US12054526B2ActiveUtilityA1
Polypeptides, nucleic acid molecules, compositions, and related methods
Est. expiryJun 15, 2038(~11.8 yrs left)· nominal 20-yr term from priority
A61K 38/17C12N 5/16A61K 38/00C07K 14/4716C07K 14/47
53
PatentIndex Score
0
Cited by
104
References
27
Claims
Abstract
Some embodiments of the invention include polypeptides comprising a myomerger polypeptide or an extracellular myomerger polypeptide. Other embodiments of the invention include nucleic acid molecules encoding polypeptides comprising a myomerger polypeptide or an extracellular myomerger polypeptide. Other embodiments of the invention include vectors comprising the nucleic acid molecule. Yet other embodiments of the invention include methods of using a myomerger polypeptide or an extracellular myomerger polypeptide. Additional embodiments of the invention are also discussed herein.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A method for lysing a liposome or a cell selected from the group consisting of an animal cell or a bacterial cell, comprising
contacting the liposome or the cell with an isolated extracellular myomerger polypeptide selected from the group consisting of SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, and SEQ ID NO: 24 or a composition comprising the isolated extracellular myomerger polypeptide, a nucleic acid molecule encoding the isolated extracellular myomerger polypeptide, or a vector comprising the nucleic acid molecule, and
lysing the liposome or the cell as a result of the contacting step, wherein the composition does not comprise myomaker polypeptide or a nucleic acid molecule encoding myomaker polypeptide.
2. The method of claim 1 , wherein the method is for lysing the cell and the cell is a mammalian cell.
3. The method of claim 1 , wherein the method is for lysing the cell and the cell is a bacterial cell or a mammalian cell.
4. The method of claim 1 , wherein the method is for lysing the cell and the cell is a gram-positive bacterial cell or a gram-negative bacterial cell.
5. The method of claim 1 , wherein the method is for lysing the cell and the cell is a cancer cell.
6. The method of claim 1 , wherein the method is for lysing the cell and the cell is a cancer cell and the cancer cell is a tumor cell.
7. The method of claim 1 , wherein the contacting occurs in vitro.
8. The method of claim 1 , wherein the contacting occurs in vivo.
9. The method of claim 1 , wherein the contacting comprises an injection.
10. The method of claim 1 , wherein the method results in one or more pores in the cell membrane or the liposome membrane.
11. The method of claim 1 , wherein the method comprises contacting the cell or the liposome with the isolated extracellular myomerger polypeptide or a composition comprising the isolated extracellular myomerger polypeptide.
12. The method of claim 11 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 19.
13. The method of claim 11 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 20.
14. The method of claim 11 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 21.
15. The method of claim 11 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 22.
16. The method of claim 11 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 23.
17. The method of claim 11 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 24.
18. The method of claim 1 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 19.
19. The method of claim 1 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 20.
20. The method of claim 1 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 21.
21. The method of claim 1 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 22.
22. The method of claim 1 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 23.
23. The method of claim 1 , wherein the isolated extracellular myomerger polypeptide is SEQ ID NO: 24.
24. The method of claim 1 , wherein the nucleic acid molecule is included in a vector, a viral vector, or a plasmid.
25. The method of claim 1 , wherein the amount of the isolated extracellular myomerger polypeptide, the nucleic acid molecule, or the vector is from about 0.0001% (by weight total composition) to about 99%.
26. The method of claim 1 , wherein the composition is a pharmaceutical composition.
27. The method of claim 1 , wherein (a) the composition is a pharmaceutical composition and (b) the amount of the isolated extracellular myomerger polypeptide, the nucleic acid molecule, or the vector is from about 0.0001% (by weight total composition) to about 50%.Join the waitlist — get patent alerts
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